Radiofrequency fusion of cardiac tissue

ABSTRACT

A method for cardiac surgical intervention relies on sealing or fusing heart valve leaflets without requiring implanted materials such as sutures or staples. The method provides a forceps having at least one shaft and an end effector assembly attached thereto. The end effector assembly includes a pair of opposing jaw members configured to move from an open, spread position to a closed, grasping position; creating at least one opening in the patient for inserting the forceps therein; inserting through the opening and manipulating jaw members of the forceps to grasp a portion of a first heart valve leaflet and a portion of a second heart valve leaflet therebetween; activating the forceps to close the jaw members about the leaflet portions under a working pressure, applying radiofrequency energy to the jaw members to seal the portion of the first heart valve leaflet to the portion of the second heart valve leaflet.

CROSS-REFERENCE TO RELATED APPLICATION

This application claims the benefit of priority of, and is a continuation of, U.S. patent application Ser. No. 11/807,251 filed on May 25, 2007, published on Apr. 3, 2008 as U.S. Patent Application Publication No. 2008/0082100 A1, “RADIOFREQUENCY FUSION OF CARDIAC TISSUE”, by Orton et al., now U.S. Pat. No. 8,070,746, “RADIOFREQUENCY FUSION OF CARDIAC TISSUE”, issued on Dec. 6, 2011, which claims priority to U.S. Provisional Patent Application No. 60/848,959 by Moses et al., filed on Oct. 3, 2006, entitled “RADIOFREQUENCY FUSION OF CARDIAC TISSUE”, the entire contents of each of which is incorporated by reference herein.

BACKGROUND

1. Technical Field

The present disclosure relates to methods and apparatuses for repairing and/or altering cardiac tissue such as a valve, including valve leaflets such as coapting valve leaflets.

2. Background

Surgical procedures such as heart valve repair and/or replacement are effective in treating heart valve incompetence (regurgitation, insufficiency) and/or damaged heart valves. However, such techniques are problematic in that invasive surgery is required to reach the valves with a surgical instrument. For example, in order to perform mitral valve surgery, a surgeon may be required to make large openings in the chest to access the mitral valve through a left atriotomy. Further, one or more large openings in the chest may be needed to cannulate the aorta and vena cavae to manipulate surgical instruments, to stop the heart during a cardiac procedure, and to repair or replace a heart valve. Such procedures result in significant trauma and metabolic derrangment to the patient and may not be appropriate for some patients such as the elderly, or patients with significant cardiac disease and/or other diseased states.

Currently, open surgical repair of damaged or incompetent heart valves employs a variety of techniques including annuloplasty rings, excision of damaged or prolapsing leaflets, transfer of chordae tendinae, artificial chordae tendinae, and edge-to-edge leaflet repair. Some of these methods for open surgical heart valve repair may be amendable to less invasive approaches such as beating heart surgery, minimally invasive surgery, thorascopic surgery, or endovascular approaches. One technique for open surgical valve repair in particular, known as the Alferi or edge-to-edge repair, might be accomplished by less invasive approaches. The edge-to-edge repair involves the fusion of opposing (facing) valve leaflets to correct valve incompetence secondary to leaflet prolapse. Current methods for edge-to-edge repair employ either classic surgical suturing with suture materials or surgical staples to accomplish leaflet fusion.

SUMMARY

The present disclosure relates to methods for fusing and/or sealing, adhering or binding heart valve leaflets or portions thereof together with or without opening the chest of a patient, with or without opening or stopping the heart, and/or with or without cardiopulmonary bypass (i.e., open-heart surgery). Such methods include the step of providing a forceps having at least one shaft and an end effector assembly attached thereto. The end effector assembly includes a pair of opposing jaw members configured to move from an open, spread position to a closed, grasping position. The method also includes the steps of creating at least one opening in the patient for inserting the forceps therein and inserting the forceps through the at least one opening to gain access to the cardiac chambers and heart valves. The method also includes the steps of manipulating the jaw members of the forceps through the at least one opening to grasp a portion of a first heart valve leaflet and a portion of a second heart valve leaflet therebetween; activating the forceps to close the jaw members about the leaflet portions under a working pressure sufficient to fuse or seal the first heart valve leaflet to the second heart valve leaflet when radiofrequency energy is applied to the jaw members; and applying radiofrequency energy to the jaw members to fuse or seal the portion of the first heart valve leaflet to the portion of the second heart valve leaflet.

In some embodiments, the at least one opening may be created in at least one of the left femoral artery, the right femoral artery, left femoral vein and right femoral vein. At least one opening may be created into the patient's chest through at least one intercostal space, sternum, diaphragm, or thoracic inlet into the pleural space or mediastinal space. In one embodiment, at least one opening is created through at least a portion of one ventricle and/or one atrium. The method may further include the step of introducing a viewing scope at least partially through the at least one opening. In one embodiment, each jaw member may include an electrically conductive sealing plate adapted to connect to an energy source and configured to communicate energy through tissue held therebetween. At least one of the electrically conductive sealing plates may include at least one stop member disposed thereon for controlling the gap distance between the jaw member within the range of about 0.001 inches (about 0.025 millimeters) to about 0.006 inches (about 0.152 millimeters), or preferably about 0.002 inches (about 0.051 millimeters) to about 0.010 inches (about 0.254 millimeters) for large tissue structures.

The present disclosure relates particularly to a method for treating mitral valve incompetence or regurgitation by fusing or sealing the anterior and posterior mitral valve leaflets within the chest of a patient. The method includes the steps of creating an opening in the patient for inserting a radiofrequency device into the heart of the patient; inserting the radiofrequency device within the opening; engaging a first portion of a mitral valve leaflet and a second portion of the mitral valve leaflet between a pair of jaw members of the radiofrequency device; closing the jaw members under a working pressure; and applying radiofrequency energy to the jaw members to seal the first portion and the second portion of the mitral valve leaflet. The method may be implemented wherein each jaw member includes an electrically conductive sealing plate adapted to connect to an energy source and configured to communicate energy through tissue held therebetween. At least one of the electrically conductive sealing plates may include at least one stop member disposed thereon for controlling the gap distance between said jaw member within the range of about 0.001 inches (about 0.025 millimeters) to about 0.006 inches (about 0.152 millimeters). Other gap distance ranges are also contemplated for large tissue structures, e.g., from about 0.002 inches (0.051 millimeters) to about 0.010 inches (about 0.254 millimeters).

These and other aspects of this disclosure will be evident upon reference to the following detailed description.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a cross-section view of the heart showing an approach for a radiofrequency device either to the mitral valve in the left ventricle or to the tricuspid valve in the right ventricle in accordance with one embodiment of the present disclosure;

FIG. 2 is a front view of a patient, showing an incision and an opening in the diaphragm for a radiofrequency device in accordance with one embodiment of the present disclosure;

FIG. 3A is a cut-away view of a heart, viewed from the base of the heart taken along section 3A-3A of FIG. 1, with the atria cut away to view the valves, with a mitral valve prior to repair in accordance with an embodiment of the present disclosure;

FIG. 3B is a cut-away view of a heart, viewed from the base of the heart, with the atria cut away to view the valves, while the mitral valve is being repaired in accordance with an embodiment of the present disclosure;

FIG. 3C is a view along section 3C-3C of FIG. 3B showing a radiofrequency device in a closed position for mitral valve repair;

FIG. 3D is a cut-away view of a heart, viewed from the base of the heart, with the atria cut away to view the valves, and a fused mitral valve repaired in accordance with the method according to an embodiment of the present disclosure;

FIG. 3E is a cut-away view of a heart, viewed from the base of the heart, with the atria cut away to view the valves, and a mitral valve fused at two treatment sites in accordance with one particular method according to an embodiment of the present disclosure;

FIG. 3F is a cut-away view of a heart, viewed from the base of the heart, with the atria cut away to view the valves, and a mitral valve in need of repair;

FIG. 3G is a cut-away view of a heart, viewed from the base of the heart, with the atria cut away to view the valves, and the mitral valve of FIG. 3F repaired in accordance with a particular method of the present disclosure;

FIG. 4A is a perspective view of an endoscopic bipolar forceps suitable for use with a particular method of the present disclosure;

FIG. 4B is a perspective view of an open bipolar forceps suitable for use with a particular method of the present disclosure; and

FIG. 5 is a greatly enlarged view of the end effector assembly of the forceps shown in FIG. 4A.

DETAILED DESCRIPTION

Methods in accordance with the present disclosure seal, fuse, repair and/or alter one or more portions of a valve together to fix a valve and/or reduce valve regurgitation. As used herein, the terms “seal” and “fuse” or “sealing” and “fusing” or “sealed” and “fused” are used interchangeably as being equivalent. The foregoing terms are defined herein also as referring normally only to partial sealing or fusing of heart valve leaflets, as opposed to complete sealing or fusing of the same, but are not limited in either respect.

Referring now to FIG. 1, a heart 30 is illustrated in a cut-away anterior view illustrating the left atrium 2 and left ventricle 4, with mitral valve 42 disposed therebetween to allow blood (not shown) to move from the left atrium 2 into the left ventricle 4, and also illustrating the right atrium 6 and right ventricle 8, with tricuspid valve 40 disposed therebetween to allow blood (not shown) to move from the right atrium 6 into the right ventricle 8. As discussed below with respect to FIG. 3A, the heart 30 also includes the aortic valve 38 that allows the blood to move out of the left ventricle 4 via the aortic arch 10 to flow to the body (not shown) and the pulmonary valve 36 that allows the blood, flowing from the body via the superior vena cava 12 and inferior vena cava 14, to move from the right ventricle 8 to the lungs (not shown) via the pulmonary trunk 16 leading to the right and left pulmonary arteries 18 a and 18 b, respectively. An endoscopic radiofrequency device 26 is also visible, which in this embodiment is disposed in an open configuration, approaching the mitral valve 42 prior to sealing, fusing, repairing and/or altering one or more portions of the mitral valve 42 together to treat the mitral valve 42 and/or reduce mitral valve 42 regurgitation. In addition, endoscopic radiofrequency device 26 is also shown disposed in an open configuration approaching the tricuspid valve 40 prior to sealing, fusing, repairing and/or altering one or more portions of tricuspid valve 40 together to treat tricuspid valve 40 and/or reduce tricuspid valve 40 regurgitation.

Referring also to FIG. 2, patient “P” is undergoing valve repair in accordance with an embodiment of the present disclosure, which may require an incision 22. A small incision 22 may be made in the diaphragm 52 of the patient “P” to insert the radiofrequency device 26 for mitral valve repair. The incision or opening may be about 0.5 (about 1.27 centimeters) to about 5 inches (about 12.7 centimeters) in length. After initial incision of the skin, one or more suitable medical devices may be used to navigate a path between the skin incision 22 and the heart 30 of the patient “P”. For example, imaging devices, such as an angioscope, as well as cutting and/or suturing devices may be used. Imaging devices may be placed in or on the patient to monitor the procedure. Medical devices, such as cutting and/or suturing devices may then be used to make at least one opening in a ventricle and/or atrium, including the left ventricle and left atrium. For example, opening 23 in left ventricle 4 provides direct access to the mitral valve 42 while opening 24 in right ventricle 8 provides direct access to the tricuspid valve 40 (see FIG. 1). Any suitable access methods or devices may be used to gain surgical access to the mitral valve 42, or other valve or tissue to be repaired. Methods in accordance with the present disclosure may be performed on a beating heart, thus eliminating the need for cardiopulmonary bypass. However, many embodiments may also be suitable for use in open-heart surgery techniques and/or in conjunction with use of cardiopulmonary bypass. Alternatively, some devices and methods may use one or more blood vessels to obtain access to the heart by catheterization, transvenous, or transarterial approaches. The chest 21 of the patient “P” may be open or closed depending on the devices and methods to be used for the sealing, fusing, fixing, repairing and/or altering of the heart valve tissue.

In embodiments, the heart valve such as the mitral valve 42 is accessed and the methods are applied from the ventricular side of the valve 42, or within the left ventricle 4. For example, given the anatomy and shape of the mitral valve 42, it may be difficult to apply techniques in accordance with the present disclosure from the atrial side of the heart 30, i.e., from the left atrium 2 or the right atrium 6. Accordingly, devices suitable for use with methods in accordance with the present disclosure may be passed through the apex 50 of the ventricles 4 and 8. In embodiments, such as catheter-based applications, a medical device may be passed through the femoral artery (not shown), through the aortic valve 38 into the left ventricle 4 or through a femoral vein (not shown) across the atrial septum and through the mitral orifice to fuse, seal, fix, repair and/or treat the mitral valve 42 from the ventricular side.

Referring now to FIGS. 3A-3B, heart 30 is viewed from the perspective of the base of the heart 30 (roughly, the top or cephalic part of the heart), as if the right and left atria 6 and 2, respectively, were removed. The pulmonary 36, aortic 38, tricuspid 40 and mitral 42 valves are shown, as well as the mitral valve annulus 44 and the anterior leaflet 46 and posterior leaflet 48 of mitral valve 42.

Referring also to FIG. 3C, radiofrequency device 26 contacts with at least one heart valve leaflet 46, 48. More particularly, the jaw members 110 and 120 of end effector assembly 100 of radiofrequency device 26 contact at least two portions of heart valve leaflet 46, 48 to create a treatment site 51 where a first portion 52 of heart valve leaflet 46 and a second portion 54 (see FIG. 3B) of heart valve leaflet 48 are adjacent to one another.

Radiofrequency device 26 is suitable for applying radiofrequency energy and/or pressure to the treatment site in amounts sufficient to seal or fuse the first portion 52 of heart valve leaflet 46 to the second portion of heart valve leaflet 48. For example, electrical energy in the frequency range of 300 kilohertz (kHz) to 1 megahertz (MHz) may be directly applied to one or more treatment sites 51 in amounts sufficient to seal or fuse the first portion of heart valve leaflet 46 to the second portion of heart valve leaflet 48. In addition, radiofrequency device 26 may be configured to provide pressure in amounts sufficient to effectively seal or fuse the first portion of heart valve leaflet 46 to the second portion of heart valve leaflet 48 at one or more treatment sites 51.

Referring now to FIG. 3D, treatment site 51 is shown having a site of leaflet fusion, seal, adhesion or weld 60 where heart leaflet 46 and heart leaflet 48 are sealed or fused together. As used herein, sealing, fusion, fixation or adhesion refer to the process of liquefying the tissues and ground substances in the tissues so that they reform into a fused mass with significantly reduced demarcation between the opposing tissue structures. In contrast, the term “cauterization” is defined as the use of heat to destroy tissue (also called “diathermy” or “electrodiathermy”) and the term “coagulation” is defined as a process of desiccating tissue wherein the tissue cells are ruptured and dried. Coagulation of small vessels is usually sufficient to permanently close them. Larger vessels and cardiac tissue need to be “sealed” or “fused” to assure a permanent weld. In some embodiments, treatment site 51 is positioned in or around the middle of the two heart valve leaflets 46 and 48 such that the middle portion of the mitral valve 42 is treated with a radiofrequency device, e.g., radiofrequency device 26, in accordance with the present disclosure. Referring to FIG. 3D, heart valve leaflets 46, 48 are sealed or fused together at treatment site 51, which is near the middle of leaflets 46, 48. In other embodiments (not shown), the leaflet fusion site might be offset towards one of the valve commissures.

Referring to FIG. 3E, two seals 53, 53′ are shown that were formed by methods in accordance with the present disclosure. In some embodiments, at least two treatment sites such as 51, 51′ are treated with a radiofrequency device, e.g., radiofrequency device 26, in accordance with the present disclosure. Referring to FIG. 3E, heart valve leaflets 46, 48 are fused or sealed together at two treatment sites 51, 51′. In some embodiments, a surgeon can apply a plurality of fusions or seals to one or more tissues, such as mitral valve leaflets. For example, the surgeon, upon having access to the heart 30, may freely position the radiofrequency device 26 at a plurality of treatment sites and activate the device 26 in accordance with the present disclosure to create a plurality of fusions or seals.

Referring to FIG. 3F, a worn heart valve leaflet 46 is shown having a lesion 71 therein. Lesion 71 is problematic in that it prevents the mitral valve 42 from functioning normally and allows blood to incorrectly flow backwards into the atrium 2 when the heart 30 is pumping. In some embodiments, a surgeon may use methods in accordance with the present disclosure to seal lesion 71 and improve the performance of leaflet 46. For example, through catheterization, a surgeon can apply the radiofrequency device 26 to the leaflet of a beating heart and treat lesions or worn valves or components thereof. FIG. 3G shows the heart 30 of FIG. 3F after application of a radiofrequency device, e.g., radiofrequency device 26, in accordance with the present disclosure to seal lesion 71. The tissue 72 has fused and the performance of the leaflet is improved.

Referring now to FIG. 4A and FIG. 4B, two bipolar forceps 10 and 10′, respectively, are shown; a first forceps 10 may be used with endoscopic surgical procedures and a second forceps 10′ for use with open surgical procedures. An endoluminal device (not shown), may also be utilized for the purposes herein. For the purposes herein, either an endoscopic instrument or an open instrument may be utilized for radiofrequency procedures in accordance with the present disclosure. Obviously, different electrical and mechanical connections and considerations apply to each particular type of instrument; however, the novel aspects with respect to the sealing, fusing, repairing and/or altering cardiac tissue such as a valve, and its operating characteristics remain generally consistent with respect to the endovascular, endoscopic or open designs of FIGS. 4A and 4B, respectively. Forceps 10 and 10′ are shown by way of example and other electrosurgical forceps are also envisioned that may support the methods in accordance with the present disclosure. In the drawings and in the description that follows, the term “proximal”, as is traditional, will refer to the end of the forceps 10, 10′ that is closer to the user, while the term “distal” will refer to the end that is further from the user.

FIG. 4A shows one example of an endoscopic vessel sealing instrument 10 which is configured to seal, repair and/or alter cardiac tissue such as a valve. More particularly, forceps 10 generally includes a housing 20, a handle assembly 50, a rotating assembly 80, a trigger assembly 70 and the end effector assembly 100 which mutually cooperate to grasp, seal and, if warranted, divide tissue. The forceps 10 includes a shaft 12 which has a distal end 9 dimensioned to mechanically engage the end effector assembly 100 and a proximal end 14 which mechanically engages the housing 20 proximate the rotating assembly 80.

Forceps 10 also includes a plug (not explicitly shown) which connects the forceps 10 to a source of electrosurgical energy, e.g., an electrosurgical generator (not shown) via an electrical cable 310. Handle assembly 50 includes a fixed handle 50 a and a movable handle 40. Handle 40 moves relative to fixed handle 50 to actuate the end effector assembly 100 and enable a user to grasp and manipulate cardiac tissue such as a valve. More particularly, the end effector assembly 100 includes a pair of opposing jaw members 110 and 120 which move in response to movement of the handle 40 from an open position wherein the jaw members 110 and 120 are disposed in spaced relation relative to one another, to a clamping or closed position wherein the jaw members 110 and 120 cooperate to grasp tissue therebetween.

The housing 20 encloses a drive assembly (not shown in FIG. 4A) which cooperates with the movable handle 40 to impart movement of the jaw members 110 and 120 from the open position to the clamping or closed position. The handle assembly 30 can generally be characterized as a four-bar mechanical linkage which provides a unique mechanical advantage when fusing or sealing tissue between the jaw members 110 and 120. For example, once the desired position for the fusing or sealing site is determined and the jaw members 110 and 120 are properly positioned, handle 40 may be compressed fully to lock the jaw members 110 and 120 in a closed position against the tissue. Further, should it be determined that tissue should be divided, trigger assembly 70 may be compressed to actuate a blade assembly (not explicitly shown) located in the end effector assembly 100. Other force activating assemblies and trigger mechanisms are envisioned which may be used in connection with the blade assemblies described herein. The details relating to the inter-cooperative relationships of the inner-working components of various forceps 10 are disclosed in commonly-owned U.S. patent application Ser. No. 10/284,562, now U.S. Pat. No. 7,267,677, “VESSEL SEALING INSTRUMENT”, issued Sep. 11, 2007 to Johnson et al., U.S. patent application Ser. No. 10/460,926, now U.S. Pat. No. 7,156,846, “VESSEL SEALER AND DIVIDER FOR USE WITH SMALL TROCARS AND CANNULAS”, issued Jan. 2, 2007 to Dycus et al., and U.S. patent application Ser. No. 10/369,894, now U.S. Patent Application Publication No. US 2003/0229344 A1, “VESSEL SEALER AND DIVIDER AND METHOD OF MANUFACTURING SAME”, by Dycus et al., published Dec. 11, 2003. When the jaw members 110 and 120 are fully compressed about the tissue, the forceps 10 is now ready for selective application of electrosurgical energy and/or tissue fusion, repair and/or alteration.

The gap distance between jaw members must be regulated to assure a consistent and reliable seal. At least one of the jaw members includes one or more stop members on a conductive surface thereof which regulates the gap distance to about 0.001 inches (about 0.025 millimeters) to about 0.006 inches (about 0.152 millimeters). Other gap distance ranges are also contemplated for large tissue structures, e.g., from about 0.002 inches (about 0.051 millimeters) to about 0.010 inches (about 0.254 millimeters).

As best seen in FIG. 5, jaw member 120 includes a series of stop members 750 preferably disposed on the inner facing surfaces of the electrically conductive sealing surface 111 to facilitate gripping and manipulation of tissue and to define a gap between opposing jaw members 110 and 120 during sealing, fusing, repairing and/or altering of cardiac tissue such as heart valve leaflets. It is envisioned that the series of stop members 750 may be employed on one or both jaw members 110 and 120 depending upon a particular purpose or to achieve a desired result. A detailed discussion of these and other envisioned stop members 750 as well as various manufacturing and assembling processes for attaching and/or affixing the stop members 750 to the electrically conductive sealing or fusing surfaces 111, 112 are described in commonly-assigned, co-pending U.S. application Ser. No. 10/471,818 entitled “VESSEL SEALER AND DIVIDER WITH NON-CONDUCTIVE STOP MEMBERS” by Dycus et al, now U.S. Pat. No. 7,473,253 published Jan. 6, 2009.

An open forceps 10′ for use in connection with traditional open surgical procedures is shown by way of example in FIG. 4B. Open forceps 10′ includes a pair of elongated shaft portions 120 a′, 120 b′ each having a proximal end 160 a′and 160 b′, respectively, and a distal end 140 a′ and 140 b′, respectively. The forceps 10′ includes jaw assembly 900′ which attaches to the distal ends 140 a′ and 140 b′ of shafts 120 a′ and 120 b′, respectively. Jaw assembly 900′ includes an upper jaw member 110′ and a lower jaw member 120′ which are movable relative to one another to grasp tissue therebetween.

Still referring to FIG. 4B, each shaft 120 a′ and 120 b′ includes a handle 170 a′ and 170 b′ disposed at the proximal end 160 a′ and 160 b′ thereof which each define a finger hole 180 a′ and 180 b′, respectively, therethrough for receiving a finger of the user. As can be appreciated, finger holes 18 a′ and 18 b′ facilitate movement of the shafts 120 a′ and 120 b′ relative to one another which, in turn, pivot the jaw members 110′ and 120′ from the open position wherein the jaw members 110′ and 120′ are disposed in spaced relation relative to one another for manipulating tissue to a clamping or closed position wherein the jaw members 110′ and 120′ cooperate to grasp tissue therebetween.

A ratchet 30 is included for selectively locking the jaw members 110′ and 120′ relative to one another at various positions during pivoting. In embodiments, each position associated with the cooperating ratchet interfaces 30 holds a specific, i.e., constant, strain energy in the shaft members 120 a′ and 120 b′ which, in turn, transmits a specific closing force to the jaw members 110′ and 120′. It is envisioned that the ratchet 30 may include graduations or other visual markings which enable the user to easily and quickly ascertain and control the amount of closure force desired between the jaw members 110′ and 120′. One of the shafts, e.g., 120 b′, includes a proximal shaft connector/flange 19′ which is designed to connect the forceps 100′ to a source of RF energy (not shown) via an electrosurgical cable 310 and plug 300. The details relating to the inner-working electrical connections and various envisioned forceps 10′ are disclosed in commonly-owned U.S. patent application Ser. No. 10/962,166, U.S. patent application Ser. No. 10/991,157, now U.S. Pat. No. 7,131,970, “OPEN VESSEL SEALING INSTRUMENT WITH CUTTING MECHANISM”, issued Nov. 7, 2006 to Moses et al., and U.S. patent application Ser. No. 10/873,860, now U.S. Patent No. 7,252,667, “OPEN VESSEL SEALING INSTRUMENT WITH CUTTING MECHANISM AND DISTAL LOCKOUT”, issued Aug. 7, 2007 to Moses et al.

As mentioned above, two mechanical factors play an important role in determining the resulting thickness of the fused or sealed tissue and effectiveness of the fusion or seal, i.e., the pressure applied between opposing jaw members 110′ and 120′ and the gap (about 0.001 to about 0.006 inches, or about 0.025 to about 0.152 millimeters) between the opposing jaw members 110′ and 120′ during the fusing or sealing process. Other gap distance ranges are also contemplated for large tissue structures, e.g., from about 0.002 inches (0.051 millimeters) to about 0.010 inches (about 0.254 millimeters). Applying the correct force is also important for other reasons: to reduce the impedance of the tissue to a low enough value that allows enough current through the tissue; and to overcome the forces of expansion during the heating of the tissue in addition to contributing towards creating the required fusion or seal thickness necessary for a good fusion or seal.

For the purposes herein, electrode assemblies 100 and 900′ include the same general configuration and are designed so that surgeons can more readily and more easily produce consistent, high quality tissue transections while limiting movement of the end effector assembly. By controlling the intensity, frequency and duration of the RF energy applied to the tissue, the user can selectively seal the tissue as needed for a particular purpose. As can be appreciated, different tissue types and the physical characteristics associated with each tissue type may require different electrical fusing or sealing and/or cutting parameters.

The present methods in accordance with the present disclosure may be applied to any blood vessel to treat tissue therein. As used herein, the word “treat,” “treating” or “treatment” refers to using the methods of the present disclosure prophylactically to prevent any undesirable conditions, or therapeutically to ameliorate an existing undesirable condition. A number of different treatments are now possible, which reduce and/or eliminate undesirable conditions.

As used herein, “undesirable condition” refers to any detectable tissue manifestations that require surgical intervention. Such manifestations can appear due to a number of factors such as, for example, trauma and/or other diseased or dysfunctional state. Non-limiting examples of such manifestations include stenosis, regurgitation, and/or other forms of tissue abnormality such as a tear or lesion in the heart, and combinations thereof. The listed undesirable conditions are non-limiting and only a portion of the conditions suitable for treatment in accordance with the present disclosure are listed herein.

In some embodiments, methods in accordance with the present disclosure apply pressure and/or radiofrequency energy in an effective amount to improve undesirable conditions. As used herein, “effective amount” refers to an amount of pressure and/radiofrequency energy needed to obtain a positive benefit by sealing or fusing tissue to repair and/or alter tissue including cardiac tissue such as a valve, corresponding valve leaflets, and combinations thereof. The positive benefit can be health-related. In embodiments, the positive benefit is achieved by sealing or fusing tissue to repair and/or alter tissue during heart surgery for heart valve repair and/or replacement.

The positive benefits can reduce, alleviate, or cure regurgitation by sealing or fusing and/or altering the valve structures to allow the valve to close tightly, or to facilitate procedures where a prosthetic ring is inserted to reshape a deformed valve. Accordingly, the positive benefit can be achieved by altering the valve flaps to stop blood from flowing backwards. A positive benefit can be achieved in that the methods in accordance with the present disclosure may be suitable for some patients that otherwise were not suitable surgical candidates. Other positive benefits of the methods in accordance with the present disclosure include lowering the risk of infection during and/or after surgery, decreasing a need for life-long blood thinner medications and/or preserving heart muscle strength.

A positive benefit may be achieved by fusion of the anterior mitral valve leaflet to the posterior mitral valve leaflet. For example, two different leaflets may be joined to one another.

A patient suffering from regurgitation for failure of a mitral valve to close tightly, may be prepared for cardiac surgery in a conventional manner using conventional techniques and procedures. The patient may be anesthetized and ventilated using conventional techniques. The surgeon prepares an opening to the heart by incising the thoracic wall or sternum with a scalpel. The surgeon next obtains access to the mitral valve through a left atriotomy and/or surgical incision through the left ventricle, and locates a worn leaflet. The surgeon performs a surgical procedure that applies radiofrequency energy and/or pressure to the worn leaflet to fuse or seal and/or reshape the leaflet.

During the surgical procedure, the surgeon optionally elects to have the patient's heart beating to perform a conventional beating heart procedure, although the surgeon has a cardiopulmonary bypass (CBP) machine primed and available if it is necessary to convert the beating heart procedure into a conventional stopped heart procedure. In this application, the instrument may be passed through a small incision in the atrium or ventricle using surgical techniques to control hemorrhage while the instrument is passed across the cardiac wall. In this application, visualization of the heart valve or cardiac structure may be obtained by echocardiography or other suitable imaging technologies.

The patient recovers and has no additional regurgitation.

As can be appreciated from the above description, referring to FIGS. 1-5, the method for sealing heart valve leaflets, e.g., anterior leaflet 46 and posterior leaflet 48 of mitral valve 42, within the chest 21 of the patient “P” includes the steps of providing a forceps, e.g., forceps 10 (see FIG. 4A) or forceps 10′ (see FIG. 4B), having at least one shaft, e.g., shaft 12 of forceps 10 or shafts 120 a′ and 120 b′ of forceps 10′, and an end effector assembly attached thereto, e.g., end effector assembly 100 of forceps 10 9 (see FIG. 4A) or jaw assembly 900′ of forceps 10′ (see FIG. 4B). The end effector assembly includes a pair of opposing jaw members configured to move from an open, spread position to a closed, grasping position, e.g., jaw members 110 and 120 of forceps 10 in FIGS. 1, 3C, 4A and 5, and jaw members 110′ and 120′ of forceps 10′ in FIG. 4B. The method includes creating at least one opening in the patient for inserting the forceps 10 therein, e.g., openings 23 and 24 in FIG. 1 and incision 22 in the left thorax of the patient “P”. The method includes inserting the forceps 10 through the at least one opening, e.g., incision 22 or openings 23 or 24. The method also includes manipulating the jaw members, e.g., jaw members 110 and 120 of the forceps 10, or jaw members 110′ and 120′ of forceps 10′, through the at least one opening, e.g., incision 22 or openings 23 or 24, to grasp a portion of a first heart valve leaflet and a portion of a second heart valve leaflet therebetween, e.g., treatment site 51 of anterior valve leaflet 46 and treatment site 51 of posterior valve leaflet 48. The method also includes activating the forceps, e.g., forceps 10 or 10′, to close the jaw members, e.g., jaw members 110 and 120 of the forceps 10, or jaw members 110′ and 120′ of forceps 10′, about the leaflet portions under a working pressure sufficient to fuse the first heart valve leaflet, e.g., anterior valve leaflet 46, to the second heart valve leaflet, e.g., posterior valve leaflet 48, when radiofrequency energy is applied to the jaw members, and applying radiofrequency energy to the jaw members, e.g., jaw members 110 and 120, or 110′ and 120′, to seal the portion of first heart valve leaflet 46 to the portion of the second heart valve leaflet 48, e.g., treatment site 51 of anterior valve leaflet 46 and treatment site 51 of posterior valve leaflet 48.

In one embodiment, each jaw member, e.g., jaw members 110 and 120 of forceps 10 and jaw members 110′ and 120′ of forceps 10′, includes an electrically conductive sealing or fusing plate, e.g., electrically conductive fusing surface 111 or 112 (see FIGS. 4A and 5) adapted to connect to an energy source and configured to communicate energy through tissue held therebetween. At least one of the electrically conductive plates 111 and 112 includes at least one stop member, e.g., stop member 750 disposed thereon for controlling the gap distance between the jaw members 110 and 120, or 110′ and 120′, within the range of about 0.001 inches (about 0.025 millimeters) to about 0.006 inches (about 0.152 millimeters). Other gap distance ranges are also contemplated for large tissue structures, e.g., from about 0.002 inches (about 0.051 millimeters) to about 0.010 inches (about 0.254 millimeters).

Referring to FIGS. 1 and 3D, as can also be appreciated from the above description, the present disclosure describes a method of treating mitral valve regurgitation by fusing or sealing cardiac mitral valve leaflets, e.g., anterior valve leaflet 46 and posterior valve leaflet 48, within the chest 21 of the patient “P”. The method includes the steps of creating at least one opening, e.g., opening or incision 22 and/or opening 23 in the left ventricle 4 (or opening 24 in the right ventricle 8 for access to for treating the tricuspid valve 40) in the patient “P” for inserting a radiofrequency device, e.g., radiofrequency device 26, into the heart 30 of the patient “P” and inserting the radiofrequency device, e.g., radiofrequency device 26, within the opening, e.g., opening or incision 22 and/or opening 23 in the left ventricle 4 (or opening 24 in the right ventricle 8 for treating the tricuspid valve 40). The method includes also engaging a first portion of a mitral valve leaflet and a second portion of the mitral valve leaflet, e.g., portions 52 and 54 of the mitral valve leaflet, e.g., anterior leaflet 46 or posterior leaflet 48, between a pair of jaw members of the radiofrequency device, e.g., jaw members 110 and 120 of the forceps 10, or jaw members 110′ and 120′ of forceps 10′. The method includes closing the jaw members, e.g., jaw members 110 and 120 of the forceps 10, or jaw members 110′ and 120′ of forceps 10′, under a working pressure and applying radiofrequency energy to the jaw members to seal the first portion 52 and the second portion 54 of the mitral valve leaflet, e.g. anterior valve leaflet 46 and posterior valve leaflet 48.

While several embodiments of the disclosure have been described, it is not intended that the disclosure be limited thereto, as it is intended that the disclosure be as broad in scope as the art will allow and that the specification be read likewise. Therefore, the above description should not be construed as limiting, but merely as exemplifications of embodiments. Those skilled in the art will envision other modifications within the scope and spirit of the claims appended hereto. 

What is claimed is:
 1. A method for sealing a first deformed heart valve leaflet having a prosthetic ring inserted therearound and a second heart valve leaflet, the method comprising: creating at least one opening in the patient; grasping a portion of a first deformed heart valve leaflet and a portion of a second heart valve leaflet therebetween; applying a working pressure sufficient to seal the first deformed heart valve leaflet to the second heart valve leaflet when radiofrequency energy is applied thereto; and applying radiofrequency energy to seal the portion of the first deformed heart valve leaflet to the portion of the second heart valve leaflet.
 2. The method according to claim 1, wherein the at least one opening is created in at least one of the left femoral artery, the right femoral artery, the left femoral vein, the right femoral vein, and combinations thereof.
 3. The method according to claim 1, wherein the at least one opening is created through at least a portion of one of a ventricle and an atrium.
 4. The method according to claim 1, further comprising the step of introducing a viewing scope at least partially through the at least one opening.
 5. The method according to claim 1, wherein the at least one opening is created in the patient's chest through at least one intercostal space, sternum, thoracic inlet, or diaphragm.
 6. The method according to claim 1, further comprising: providing a forceps having at least one shaft and an end effector assembly attached thereto, the end effector assembly including a pair of opposing jaw members configured to move from an open, spread position to a closed, grasping position; inserting the forceps through the at least one opening; manipulating the jaw members of the forceps through the at least one opening to grasp the portion of the first deformed heart valve leaflet and the portion of the second heart valve leaflet therebetween; connecting an energy source to an electrically conductive sealing plate included on each jaw member to enable radiofrequency energy to be applied to the jaw members; activating the forceps to close the jaw members about the leaflet portions under the working pressure sufficient to seal the portion of the first deformed heart valve leaflet to the portion of the second heart valve leaflet when radiofrequency energy is applied to the jaw members; and controlling a gap distance between said jaw members via at least one stop member disposed thereon.
 7. The method according to claim 6, wherein the step of controlling the gap distance between the jaw members includes controlling the gap distance within a range of about 0.001 inches (about 0.025 millimeters) to about 0.006 inches (about 0.152 millimeters).
 8. The method according to claim 6, wherein the step of controlling the gap distance between the jaw members includes controlling the gap distance within a range of about 0.002 inches (about 0.051 millimeters) to about 0.010 inches (about 0.254 millimeters).
 9. A method of treating, within the chest of a patient, mitral valve regurgitation by fusing first and second portions of a cardiac mitral valve leaflets, the method comprising: creating an opening in the patient for inserting a radiofrequency device into the heart of the patient; inserting the radiofrequency device having opposing jaw members within the opening; engaging between the pair of jaw members of the radiofrequency device a first portion of a mitral valve leaflet and a second portion of the mitral valve leaflet, at least one of the first and second portions of the mitral valve leaflet including a prosthetic ring disposed therearound; closing the jaw members under a working pressure sufficient to seal the first portion and the second portion of the mitral valve leaflet; and applying radiofrequency energy to the jaw members to seal the first portion and the second portion of the mitral valve leaflet.
 10. The method according to claim 9, further comprising: connecting an energy source to an electrically conductive sealing plate included on each jaw member to enable radiofrequency energy to be applied to the jaw members; closing the jaw members about the first and second portions of the mitral valve leaflet under the working pressure sufficient to seal the first mitral valve leaflet portion to the second mitral valve leaflet portion when radiofrequency energy is applied to the jaw members; and controlling a gap distance between said jaw members via at least one stop member disposed thereon.
 11. The method according to claim 10, wherein the step of controlling the gap distance between the jaw members includes controlling the gap distance within a range of about 0.001 inches (about 0.025 millimeters) to about 0.006 inches (about 0.152 millimeters).
 12. The method according to claim 10, wherein the step of controlling the gap distance between the jaw members includes controlling the gap distance within a range of about 0.002 inches (about 0.051 millimeters) to about 0.010 inches (about 0.254 millimeters). 